Canonical Allele Identifier: CA2665985206

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293314-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293314G>C , CM000665.2:g.52293314G>C	GRCh38
NC_000003.11:g.52327330G>C , CM000665.1:g.52327330G>C	GRCh37
NC_000003.10:g.52302370G>C	NCBI36
NG_023246.1:g.10495G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*188G>C MANE Select	ENSP00000389175.2:n.*188G>C
ENST00000436784.6:c.*188G>C	ENSP00000389175.2:n.*188G>C
ENST00000471180.5:c.*66G>C	ENSP00000417526.1:n.*66G>C
ENST00000473032.5:c.*66G>C	ENSP00000418951.1:n.*66G>C
ENST00000486393.5:c.*1123G>C	ENSP00000419868.1:n.*1123G>C
ENST00000489173.1:n.1922G>C
NM_145262.3:c.*188G>C	NP_660305.2:n.*188G>C
NR_026699.1:n.1858G>C
NR_026700.1:n.850G>C
NR_026701.1:n.1742G>C
NR_026702.1:n.780G>C
XM_005264878.2:c.*879G>C	XP_005264935.1:n.*879G>C
XR_245095.2:n.2897G>C
XM_017005730.1:c.*188G>C	XP_016861219.1:n.*188G>C
XM_024453351.1:c.*188G>C	XP_024309119.1:n.*188G>C
XM_024453352.1:c.*879G>C	XP_024309120.1:n.*879G>C
XR_001740022.2:n.3548G>C
XR_001740023.2:n.3072G>C
XR_245095.4:n.2898G>C
NM_145262.4:c.*188G>C MANE Select	NP_660305.2:n.*188G>C
NR_026699.2:n.1850G>C
NR_026700.2:n.842G>C
NR_026701.2:n.1734G>C
NR_026702.2:n.772G>C
NM_001144951.2:c.*879G>C	NP_001138423.1:n.*879G>C